Skip to main content
Log in

Legionella pneumophila intracellular growth in normal vs. Immune guinea pig macrophage cultures

  • Published:
Current Microbiology Aims and scope Submit manuscript

Abstract

Intracellular growth ofLegionella pneumophila, an opportunistic intracellular bacterium considered the cause of legionellosis, was assessed in peritoneal macrophages from normal and immunized guinea pigs. These bacteria grew exceedingly well in the normal guinea pig macrophages. Uptake of these bacteria was about the same by macrophages from either normal or immune guinea pigs, but their growth in immune macrophages was completely inhibited. Macrophages from normal guinea pigs stimulated with mezerin, a compound similar to diterpene ester, a known nonspecific stimulator of macrophages, or with specificLegionella vaccine released moderate or only small amounts of hydrogen peroxide, an indicator of macrophage activation to antimicrobicidal activity. In contrast, macrophages from immune guinea pigs produced much higher levels of hydrogen peroxide when stimulated with mezerein or theLegionella vaccine, and also showed a heightened response when cultured without a stimulator. These results indicate that macrophage activation related to the immune status of the host appears to have an important role in initial resistance toLegionella growth in susceptible individuals.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Literature Cited

  1. Babior BM (1978) Oxygen-dependent microbial killing by phagocytes. N Engl J Med 298:659–668

    PubMed  Google Scholar 

  2. Bhardwaj N, Nash TW, Horwitz MA (1986) Interferon-ractivated human monocytes inhibit the intracellular multiplication ofLegionella pneumophila. J Immunol 137:2662–2669

    PubMed  Google Scholar 

  3. Brieman R and Horwitz M (1987). Guinea pigs sublethally infected with aerosolizedLegionella pneumophila develop humoral and cell mediated immune response and are protected against lethal aerosol challenge. J Exp Med 164:799–811

    Google Scholar 

  4. Eisenstein TK, Friedman H (1985) Immunity to Legionella.In: Katz SM (ed) Legionellosis, Vol II. Boca Raton, Florida: CRC Press, pp 159–169

    Google Scholar 

  5. Friedman F, Widen R, Klein T, Friedman H (1984) Lymphoid cell blastogenesis as anin vitro indicator of cellular immunity toLegionella pneumophila antigens. J Clin Microbiol 19:834–837

    PubMed  Google Scholar 

  6. Friedman H, Widen R, Klein T, Searls L, Cabrian K (1984)Legionella pneumophila-induced blastogenesis of murine lymphoid cellsin vitro. Infect Immun 43:314–319

    PubMed  Google Scholar 

  7. Gangadharam PRJ, Edwards CK III (1984) Release of superoxide anion from resident and activated mouse peritoneal macrophages infected withMycobacterium intracellulare. Am Rev Respir Dis 130:834–838

    PubMed  Google Scholar 

  8. Horwitz M, Silverstein S (1971) Interactions of the Legionnaires' disease bacteria (Legionella pneumophila, with human phagocytes I.L. pneumophila resists killing by polymorphonuclear leukocytes, antibody and complement. J Exp Med 153:386–397

    Google Scholar 

  9. Horwitz M, Silverstein S (1981) Interactions of the Legionnaires' disease bacteria (Legionella pneumophila) with human phagocytes. II. Antibody promotes binding of monocytes but does not inhibit intracellular multiplication 153:398–406

  10. Jacobs RF, Locksley RM, Wilson CB, Haas JE, Klebanoff SJ (1984) Interaction of primate alveolar macrophages andLegionella pneumophila. J Clin Invest 73:1515–1523

    PubMed  Google Scholar 

  11. Johnston RB (1981) Enhancement of phagocytosis associated oxidative metabolism as a manifestation of macrophage activation.In: Pick E (ed) Lymphokines, Vol 3. New York: Academic Press, pp 33–56

    Google Scholar 

  12. Kishimoto RA, White JD, Shirey FG, MacGann VG, Berendt RF, Larson EW, Hedlund KW (1981)In vivo response of guinea pig peritoneal macrophages toLegionella pneumophila. Infect Immun 31:1209–1213

    PubMed  Google Scholar 

  13. Lowry OH, Rosebrough NJ, Farr AL, Randall RJ (1951) Protein measurement with the Folin phenol reagent. J Biol Chem 193:265–271

    PubMed  Google Scholar 

  14. Murray HW, Juangbhanich CW, Nathan CF, Cohn ZA (1979) Macrophage oxygen-dependent antimicrobial activity. II. The role of oxygen intermediates. J Exp Med 150:950–964

    PubMed  Google Scholar 

  15. Pick E, Keisari Y (1981) Superoxide anion and hydrogen peroxide production by chemically elicited peritoneal macrophages—induction by multiple nonphagocytic stimuli. Cell Immunol 59:301–318

    PubMed  Google Scholar 

  16. Taylor JL, Sedmak J, Jameson P, Lin YG, Grossberg SE (1984) Markeldy enhanced production of gamma interferon in murine T lymphocytes treated with lentil lectin and diterpene ester, mezerein. J Interferon Res 4:315–327

    PubMed  Google Scholar 

  17. Yamamoto Y, Klein TW, Newton CA, Widen R, Friedman H (1987) Differential growth ofLegionella pneumophila in guinea pigs vs. mouse macrophage cultures. Infect Immun, in press

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Yamamoto, Y., Klein, T.W. & Friedman, H. Legionella pneumophila intracellular growth in normal vs. Immune guinea pig macrophage cultures. Current Microbiology 16, 333–336 (1988). https://doi.org/10.1007/BF01568541

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01568541

Keywords

Navigation